Flowcardia, Inc.
Flowcardia, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2010.
Top product codes for Flowcardia, Inc.
Recent clearances by Flowcardia, Inc.
- K092175 — THE CROSSER S6 CATHETER, THE CROSSER SYSTEM ELECTRONICS, MODEL CRUS6, GEN200
- K090621 — FLOWCARDIA FLOWMATER INJECTOR, MODEL INJ 100
- K091254 — THE CROSSER 14 OTW CATHETER, MODEL CRU014
- K091119 — MODIFICATION TO THE CROSSER SYSTEM
- K080849 — MICROSHEATH LP AND LP-AT
- K080765 — CROSSER LP SYSTEM
- K073289 — MICROSHEATH XL CATHETERS
- K072776 — THE CROSSER SYSTEM
- K062868 — THE CROSSER CATHETER, MODEL CR1100 AND SYSTEM ELECTRONICS, MODEL FG1002-02
- K051580 — VP SHEATH
- K051062 — VP WIRE GW140ST (.014 165CM, STANDAR), MODEL GW140ST; VP WIRE GW140SO (.014 165CM, SOFT) MODEL GW140SO
Data sourced from openFDA. This site is unofficial and independent of the FDA.